X-linked monogenic disease +
thrombophilia +

46,XY sex reversal 2
Abruzzo-Erickson syndrome
antithrombin III deficiency
cataract 40
congenital bilateral absence of vas deferens +
corpus callosum agenesis-abnormal genitalia syndrome
developmental and epileptic encephalopathy 90
dilated cardiomyopathy 3B
disseminated intravascular coagulation +
fetal akinesia deformation sequence syndrome X-linked
heparin cofactor II deficiency
McLeod syndrome
Meester-Loeys syndrome
Melnick-Needles syndrome
non-syndromic X-linked intellectual disability +
Ogden syndrome
ovarian dysgenesis 2
primary ovarian insufficiency 1
primary ovarian insufficiency 4
protein C deficiency +
protein S deficiency +
prothrombin deficiency
prothrombin thrombophilia
reducing body myopathy 1B
retinitis pigmentosa 2
retinitis pigmentosa 24
split hand-foot malformation 2
syndromic microphthalmia 1
syndromic microphthalmia 13
syndromic X-linked intellectual disability +
TARP syndrome
thrombophilia due to activated protein C resistance
thrombophilia due to decreased release of PLAT
thrombophilia due to HRG deficiency
thrombophilia due to thrombin defect
thrombophilia due to thrombomodulin defect
thrombotic thrombocytopenic purpura
X-linked cardiac valvular dysplasia
X-linked central diabetes insipidus
X-linked cleft palate with or without ankyloglossia
X-linked dilated cardiomyopathy
X-linked dominant disease +
X-linked epilepsy with variable learning disabilities and behavior disorders
X-linked exudative vitreoretinopathy 2
X-linked hereditary ataxia +
X-linked hypoparathyroidism
X-linked lissencephaly 1
X-linked lissencephaly 2
X-linked nonsyndromic deafness +
X-linked panhypopituitarism
X-linked recessive disease +
X-linked reticulate pigmentary disorder
X-linked retinitis pigmentosa and sinorespiratory infections